Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16824658 | 0.925 | 0.040 | 1 | 185895380 | intron variant | A/G | snv | 7.6E-02 | 2 | ||
rs6598902 | 0.925 | 0.040 | 1 | 27779198 | intron variant | T/C | snv | 0.18 | 2 | ||
rs693 | 0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 | 7 | |
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 6 | |||
rs887829 | 0.763 | 0.280 | 2 | 233759924 | intron variant | C/T | snv | 0.36 | 6 | ||
rs4953023 | 0.925 | 0.040 | 2 | 43846861 | non coding transcript exon variant | G/A | snv | 6.9E-02 | 5 | ||
rs4245791 | 0.882 | 0.080 | 2 | 43847292 | non coding transcript exon variant | C/A;T | snv | 4 | |||
rs6756629 | 0.925 | 0.080 | 2 | 43837951 | missense variant | G/A;T | snv | 6.7E-02 | 4 | ||
rs4148217 | 0.790 | 0.280 | 2 | 43872294 | missense variant | C/A;T | snv | 0.21; 1.2E-05 | 3 | ||
rs4148323 | 0.701 | 0.440 | 2 | 233760498 | missense variant | G/A | snv | 2.2E-02 | 9.2E-03 | 3 | |
rs6742078 | 0.807 | 0.240 | 2 | 233763993 | intron variant | G/T | snv | 0.36 | 3 | ||
rs1011770 | 0.925 | 0.040 | 2 | 159382207 | intron variant | A/G | snv | 2.5E-02 | 2 | ||
rs11887534 | 0.653 | 0.440 | 2 | 43839108 | missense variant | G/A;C | snv | 6.4E-06; 6.7E-02 | 2 | ||
rs16843641 | 0.925 | 0.040 | 2 | 159061866 | intron variant | T/C | snv | 1.2E-02 | 2 | ||
rs41360247 | 0.882 | 0.080 | 2 | 43846517 | non coding transcript exon variant | T/C | snv | 7.9E-02 | 2 | ||
rs253314 | 0.925 | 0.040 | 5 | 16871155 | intron variant | A/C | snv | 6.9E-02 | 2 | ||
rs2072183 | 0.925 | 0.040 | 7 | 44539581 | synonymous variant | G/A;C | snv | 4.0E-06; 0.25 | 3 | ||
rs2865108 | 0.925 | 0.040 | 7 | 67861752 | intergenic variant | C/A | snv | 0.89 | 2 | ||
rs10094715 | 0.925 | 0.040 | 8 | 46473341 | intergenic variant | A/G | snv | 9.8E-03 | 2 | ||
rs10888095 | 0.925 | 0.040 | 8 | 15004905 | intron variant | C/A;G | snv | 2 | |||
rs17063627 | 0.925 | 0.040 | 9 | 77424742 | intron variant | A/G | snv | 7.2E-02 | 2 | ||
rs17241442 | 0.925 | 0.040 | 9 | 115062806 | intron variant | G/A | snv | 0.11 | 2 | ||
rs41440452 | 0.925 | 0.040 | 9 | 122717961 | intergenic variant | G/A | snv | 7.9E-02 | 2 | ||
rs10998022 | 0.925 | 0.040 | 10 | 68210229 | intron variant | C/T | snv | 0.26 | 2 | ||
rs1111875 | 0.776 | 0.360 | 10 | 92703125 | intergenic variant | C/T | snv | 0.36 | 2 |